OCULAR MANIFESTATIONS OF XERODERMA PIGMENTOSUM

被引:0
|
作者
Zafar, Saemah Nuzhat [1 ]
Khan, Ayesha [1 ]
Rubab, Shehla [1 ]
Zafar, Nadeem [2 ]
机构
[1] Al Shifa Eye Hosp, Dept Histopathol, Rawalpindi, Pakistan
[2] Combined Mil Hosp, Dept Histopathol, Kharian, Pakistan
来源
JCPSP-JOURNAL OF THE COLLEGE OF PHYSICIANS AND SURGEONS PAKISTAN | 2007年 / 17卷 / 12期
关键词
Xeroderma pigmentosum; Squamous cell carcinoma; Malignant melanoma;
D O I
暂无
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Xeroderma Pigmentosum (XP) is an Autosomal Recessive (AR) condition characterized by photosensitivity and inability to repair Ultra-Violet (UV) induced DNA damage. Patients diagnosed with XP, presenting to the Paediatric Ophthalmology Department of Al-Shifa Trust Eye Hospital, Rawalpindi, were evaluated and followed-up over a period of one year, for the effects of the disease process on vision and for the development of ocular tumours. Excision of the tumours, if present, was performed under general anaesthesia. Counselling of the patients was done. Referral to oncologist and dermatologist was made, if so warranted, after histopathology of excision biopsy.
引用
收藏
页码:751 / 753
页数:3
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